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ATLA 29, 649–668, 2001 649 In Vitro Models of the Intestinal Barrier The Report and Recommendations of ECVAM Workshop 461,2 Eric Le Ferrec,3 Christophe Chesne,3 Per Artusson,4 David Brayden,5 Gérard Fabre,6 Pierre Gires,7 François Guillou,6 Monique Rousset,8 Werner Rubas9 and Maria-Laura Scarino10 3BIOPREDIC, Technopole Atalante Villejean, 14–18 rue Jean Pecker, 35000 Rennes, France; 4Department of Pharmaceutics, Biomedical Centre, Uppsala University, 751 23 Uppsala, Sweden; 5ELAN Biotechnology Research, Biotechnology Building, Trinity College, Dublin 2, Ireland; 6Sanofi Synthelabo Recherche, Departement Phamacologie & Métabolisme, 371 rue du Pr Blayac, 34184 Montpellier, France; 7Rhone Poulenc Rorer, DMPK, Preclinical Department (in vivo & in vitro), 13 Quai Jules Guesdes, 94403 Vitry Sur Seine, France; 8INSERM U178, Hopital Paul Brousse, 16 Avenue Paul Vaillant Couturier, 94807 Villejuif, France; 9GENENTECH Inc., 1 DNA Way, South San Francisco, CA 94080, USA; 10Istituto Nazionale di Ricerca per gli Alimente e la Nutrizione, Via Ardeatina 546, 00178 Rome, Italy Preface This is the report of the forty-sixth of a series of workshops organised by the European Centre for the Validation of Alternative methods (ECVAM). ECVAM’s main goal, as defined in 1993 by its Scientific Advisory Committee, is to promote the scientific and regulatory acceptance of alternative methods which are of importance to the biosciences and which reduce, refine or replace the use of laboratory animals. One of the first priorities set by ECVAM was the implementation of procedures which would enable it to become well-informed about the state-of-the-art of non-animal test development and validation and the potential for the possible incorporation of alternative tests into regulatory procedures. It was decided that this would be best achieved by the organisation of ECVAM workshops on specific topics, at which small groups of invited experts would review the current status of in vitro tests and their potential uses, and make recommendations about the best ways forward (1). In addition, other topics relevant to the Three Rs (reduction, refinement and replacement) concept of alternatives to animal experiments have been considered in several ECVAM workshops. The workshop on in vitro models of the intestinal barrier was held in Paris, France, on 4–5 March 1999. The principal aims of the workshop were to seek a consensus on the current models of the intestinal barriers and ways to screen for the movement of drugs across this barrier, and to make useful recommendations for the promotion of the Three Rs in this area. The panel of techniques used for the prediction of the relevant parameters is very large, including in vivo and in situ methods, Address for correspondence: BIOPREDIC, Technopole Atalante Villejean, 14–18 rue Jean Pecker, 35000 Rennes, France. Address for reprints: ECVAM, Institute for Health & Consumer Protection, European Commission Joint Research Centre, 21020 Ispra (VA), Italy. 1ECVAM — The European Centre for the Validation of Alternative Methods. 2This document represents the agreed report of the participants as individual scientists. E. Le Ferrec et al. 650 cell culture techniques, and in vivo studies with human volunteers. It was intended to compare these different models, and to delineate their strengths and weaknesses in the various screening situations encountered in the pharmaceutical industry. Introduction The intestinal epithelium is a gatekeeper, i.e. it controls the entry of nutrients and xenobiotics (for example, medicines). Knowledge of the absorption and metabolism of these substances at the intestinal mucosal level is of particular importance, since the oral bioavailability of a drug is defined as the fraction of an oral dose that reaches the systemic circulation. Drug absorption is considered to be a complex transfer process across the intestinal lining, which includes passive diffusion through the paracellular space and/or membranes of absorptive cells, vesicular uptake (endocytosis/pinocytosis), and release at the basolateral space (transcytosis; 2). This transport may or may not be receptor-mediated (or transportermediated), entailing uptake across the apical domain with subsequent passive diffusion into the basolateral space (Figure 1; 3). Each transport mechanism depends on the physicochemical properties of the absorbed compound, such as its stereochemistry, partition into mem- branes, molecular weight and/or size, molecular volume, pKa, solubility, chemical stability and charge distribution. Physiological factors such as gastric emptying, gastrointestinal motility, intestinal pH, blood flow, lymph flow (Figure 2), pathological state, drug interactions, nutrition, and mucus dissolution, also need to be considered when evaluating absorption (4–6). Upon ingestion, compounds have to be liberated from their dosage form, which includes dissolution into a complex medium containing numerous compounds (bile salts, ions, lipids, cholesterol and enzymes; 7). This medium can vary considerably, depending on the individual, the intestinal segment, the diet, etc. (8). Measurements of absolute solubility and dissolution are performed routinely during drug development. However, knowledge of intestinal drug dissolution is limited, due to the non-physiological aspects of in vitro systems; for example, instead of using intestinal fluid, buffer systems are commonly employed, which may result in an overestimation or underestimation of the actual events in vivo (9–12). Since the intestinal fluid is rich in enzymes derived from dying enterocytes and/or the intestinal flora, gastrointestinal stability includes both physicochemical and enzymic stability. The intestinal cell lining is covered with a viscous and elastic gel produced by the gob- Figure 1: Routes and mechanisms of transport of molecules across the intestinal epithelium 1 2 3 4 Apical membrane Tight junctions Basolateral membrane Intestinal cells Paracellular Transcellular 1) Paracellular; 2) transcellular passive diffusion; 3) transcytosis; 4) carrier-mediated uptake at the apical domain followed by passive diffusion across the basolateral membrane. ECVAM Workshop 46: the intestinal barrier 651 Figure 2: Factors influencing intestinal absorption Nutrient intake Nervous innervation Paracrine hormonal control Gastric motility Intestinal motility Dissolution or binding in mucus Nervous innervation Paracrine hormonal control Xenobiotic physical and chemical characteristics (molecular weight, pKa, solubility, chemical stability, lipophilicity etc.) Physiological factors (disease, intestinal pH etc.) Absorption (Paracellular, transcellular passive diffusion, transcellular endocytosis, transcellular carriermediated transport) Luminal factors, bacterial toxins, bile Number of enterocytes Metabolism Secretion (ions, fluid) Functional state of enterocyctes Blood and lymph flow Distribution Elimination (metabolism, excretion) From (3). let cells of the villous epithelium. The physicochemical properties of this gel can influence the rate of diffusion from the bulk to the site of absorption. Furthermore, metabolic enzymes could be associated with the mucus layer. Thus, the gel is considered to be the first in a series of absorptive barriers (13). The enzymic barrier to oral absorption could consist of several layers, depending on the properties of a compound. Also, as well as the enzymes within the intestinal lumen, there are additional enzymes located in the absorptive cells themselves, such as several cytochrome P450 (CYP) isoforms (Table I). In combination with P-glycoprotein (P-gp), these enzymes are responsible for the intestinal first-pass effect. E. Le Ferrec et al. 652 Table I: Examples of CYP expression as a function of their human intestinal localisation CYP Stomach Duodenum Ascending colon Transverse colon Descending colon 1B1 2E1 3A4 3A5 +++++ +++ +++ ++++ + ++ ++++ +++++ ++++ ++ ++ ++++ + + + +++ + +++ ++ ++ See reference (60). The number of + signs indicates the relative amount of CYP expressed The Current Models The intestinal mucosa is characterised by the presence of villi that constitute the anatomical and functional unit for nutrient and drug absorption (14). The presence of villi and microvilli provides a massive surface area for absorption (approximately 250m2 in a human). The mucosa consists of the epithelial layer, the lamina propria (collagen matrix containing blood and lymphatic vessels) and the muscularis mucosa. Therefore, any xenobiotic entering the bloodstream has to pass through the epithelial layer, part of the lamina propria, and the wall of the respective vessel. It is crucial to select an appropriate model for understanding the ratelimiting step in the absorption process. Figure 3: The place of isolated perfused organs in biomedical research Animal Experiments In situ (animals) Isolated perfused organs In vivo (human) Animal cell culture Human cell culture Monolayer, multilayer Monolayer, multilayer = predictive for; = cell/organs derived from. ECVAM Workshop 46: the intestinal barrier Three groups of methods have emerged for investigating the principal mechanisms of absorption in animals, namely, in vivo, in situ and in vitro methods. The choice of model depends totally on the questions to be answered with respect to the test compound being studied. In vivo models The main advantage of in vivo models is the integration of the dynamic components of the mesenteric blood circulation, the mucous layer and all the other factors that can influence drug dissolution. The most frequently used animal model is the rat, since it better reflects the human situation with respect to paracellular space and metabolism than the dog, which is different to the human, particularly in relation to metabolism, and overestimates the absorption of paracellularly restricted compounds (15). However, oral studies in rats also have limitations, and tend to provide false-positive results. It has therefore been stated that “the only real model for man is man” (16). Techniques such as “cassette dosing” can give global information on drug bioavailability, including intestinal barrier passage (17). This technique is useful when there are a large number of products to test (high throughput screening [HTS)], when products with good bioavailability are tested, and when organotypic in vitro models are not appropriate. The disadvantage of in vivo models is that it is impossible to separate the variables involved in the process of absorption, i.e. it is not possible to identify individual rate-limiting factors. In situ models The development of stable, vascularly perfused preparations of the small intestine has provided a powerful research tool for the investigation of intestinal transport and metabolism. In this approach, the abdominal cavity of an anaesthetised animal is exposed by laparotomy. The intestinal segment into which the drug solution is introduced can be either a closed loop or an open loop. In situ methods have significant advantages over in vivo models. For example, bypassing the stomach means that acidic compounds are not likely to precipitate, so dissolution rates do not confuse intestinal drug concentrations and therefore plasma 653 levels. Furthermore, in situ instillation allows the experimenter to assess formulation-independent breakdown in the stomach under acidic conditions. Although the animal has been anaesthetised and surgically manipulated, mesenteric blood flow is intact. However, caution must be taken with the choice of anaesthetic, since it has recently been demonstrated that anaesthesia can have strong effects on intestinal drug absorption (18). An additional consideration when using in situ techniques is the volume of the luminal drug solution, because this may change due to either absorption or secretion of water. This necessitates the use of non-absorbable or low-absorbable volume-marker compounds, such as radiolabelled poly(ethylene glycol) (PEG) 4000, inulin or mannitol, and fluorescent markers, such as lucifer yellow. It is noteworthy that the disappearance of drug from the perfusate does not always equate with absorption. Thus, it is prudent to include sampling from the portal vein, in addition to monitoring the change in perfusate concentration. By moving the sampling location from the portal vein to the hepatic vein, additional information about liver first-pass effect can be obtained. In humans, the intestinal passage of drugs can be studied by the balloon technique (Loc1-Gut), with drug administration by catheter and analysis of blood sampling (2, 19). With this technique, drug passage can be studied at various intestinal levels. This is a reference technique, but it is expensive to perform and difficult to handle; it cannot be used routinely during drug development (20). With this model, it is also possible to study compound secretion into the intestinal lumen after intravenous administration, i.e. it is feasible to investigate mediation of export of xenobiotics into the intestinal lumen by P-gp, multidrug resistance-associated protein (MRP) and lung cancer-associated resistance protein (LRP). In vitro models Organotypic models All intestinal cell types (for example, enterocytes, caliciform cells and lymphocytes) are present in organotypic models, which are used to study formulation effects (with the possible use of parenteral lipid emulsions, such as Intralipid®, or bovine serum albumin 654 for drugs having low solubility), intestinal metabolism/stability, and regional differences in permeability. Some studies have shown that permeability to various marker molecules varies along the intestinal canal. In general, permeability decreases in the order: jejunum > ileum > colon (21). The half-lives of these models are short (1–3 hours). Everted gut sac The everted gut sac of the rat small intestine can be used to determine kinetic parameters with high reliability and reproducibility (19, 22). Oxygenated tissue culture media and specific preparation techniques ensure tissue viability for up to 2 hours. The technique can be used to study drug transport across the intestine and into the epithelial cells, provided that sensitive detection methods are employed (23). Radiolabelled compounds are most appropriate. This technique was used in the past to study the transport of macromolecules and liposomes but, more recently, it was used mainly to quantify the paracellular transport of hydrophilic molecules, and to estimate the effects of potent enhancers on their absorption (23). The transport of mannitol, a paracellular marker, shows an apparent permeability (Papp) of 1.5 × 10–5 to 1.7 × 10–5 cm/s. This value is the same as those reported with low-molecular weight hydrophilic drugs in human perfusion studies. The toxicities of potential enhancers can be monitored by studying the release of intracellular enzymes or by histological examination. Molecules that cross the epithelial barrier by a transcellular route have a much higher permeability, which can also be accurately quantified by using the everted sac system. This kind of model is suitable for measuring absorption at different sites in the small intestine (24), and for performing preliminary experiments on the colon (19, 21). It is also useful for estimating the first-pass metabolism of drugs in intestinal epithelial cells. Also, by using this model (everted or not), it is convenient to study the effect of Pgp on xenobiotic transport through the intestinal barrier. A potential disadvantage of this approach is the presence of the muscularis mucosa, which is not usually removed from everted sac preparations. Therefore, this model does not reflect the actual intestinal barrier, because compounds under investigation pass E. Le Ferrec et al. from the lumen into the lamina propria (where blood and lymph vessels are found) and across the muscularis mucosa. Thus, the transport of compounds with a propensity to bind to muscle cells might be underestimated. Isolated and perfused intestinal segments During the last decade, a wide range of isolated organ systems have been developed for biomedical and pharmaceutical research. The availability of sophisticated equipment, increased manual skills, and the routine use and standardisation of models and protocols, have led to the increased reproducibility and validity of experimental results under circumstances that are virtually “true-to-life”. These methods contribute to the reduction of animal experimentation. Figure 3 shows the place of isolated perfused organs in biomedical research, compared with cell cultures of either human or animal origin. The results are recognised as predictive of the in vivo situation, including absorption at the organ level (19, 20, 25). Isolated perfused organs have the advantage that the scientist works with an intact organ, where physiological cell–cell contacts and normal intracellular matrixes are preserved (25). The major limitation is the short duration of the experiments that are possible, since changes occur rapidly. Ussing chambers Ussing chambers were introduced by Ussing & Zehran in 1951 (26) for studying the active transport of sodium as a source of electric current in short-circuited, isolated frog skin. Later on, these chambers were extensively used for the study of ion transport across many types of membrane. The usefulness of Ussing chambers for intestinal transport studies has long been recognised, and they have also been used to study the intestinal metabolism of xenobiotics (19). In this system, the drug can be exposed at either the mucosal level (apical side of enterocytes) or the serosal level (basolateral side of enterocytes). Furthermore, the simplicity of Ussing chambers makes them an attractive in vitro model system for studying drug transport. When properly equipped with electrodes, Ussing chambers are useful for studying the effects of compounds on electro-physiological parameters of the intestinal barrier. This type of study may add additional information ECVAM Workshop 46: the intestinal barrier on the pharmacological behaviour of the test compound (27). Cell models The study of absorption mechanisms is best performed in a model that contains only absorptive cells, without the confounding contributions of mucus, the lamina propria and/or the muscularis mucosa. Therefore, much attention is currently paid to the use of epithelial cell cultures for studies of drug transport mechanisms. However, the use of isolated intestinal epithelial cells has been slow to gain popularity, because they are difficult to culture and have limited viability (28–35). The development of human cell culture systems has been limited by the loss of important in vivo anatomical and biochemical features. Attention has therefore turned to the use of human adenocarcinoma cell lines, such as HT-29 and Caco-2, that reproducibly display a number of properties characteristic of differentiated intestinal cells (36). In addition, the development of these cell line models was paralleled by the development of sensitive and automated measurement techniques (for example, liquid chromatography and mass spectrometry). The limitations of cell models must not be overlooked, but they offer the advantage of relative simplicity, and are suitable for automated procedures and HTS. These cell lines originated from tumours, and are out of the in vivo physiological environment; therefore, extrapolation of the data to the in vivo situation may be difficult (as is true of most in vitro systems). Non-intestinal cell systems Madin Darby canine kidney (MDCK) cells were isolated from a dog kidney by Madin & Darby (37). They are currently used to study the regulation of cell growth, drug metabolism, toxicity and transport at the distal renal tubule epithelial level. MDCK cells have been shown to differentiate into columnar epithelial cells, and to form tight junctions when cultured on semi-permeable membranes. The use of these cells as a cellular barrier model for assessing intestinal epithelial drug transport was discussed by Cho et al. (38). The results suggested that MDCK cells, like Caco-2 cells, are suitable for molecular-permeability screening studies. Interestingly, these cells do not need 3 weeks in culture 655 before they can be used and, unlike Caco-2 cells, they do not express P-gp. Small-intestine cell lines from fetal and neonatal rats Cell lines such as IEC (39) and RIE (40) have been isolated after the repeated cloning of epithelial cells from neonatal rat small intestines. These cell lines show morphological and functional characteristics which suggest that they are derived from crypt cells (41). The IEC line was specifically employed to analyse the role of growth factors in epithelial cell physiology, and for studies on the specific functions of intestinal cells (for example, involving amino acids, glucose and nucleotide transport, or cholesterol synthesis), as well as to perform fundamental studies (36). In contrast, only a few studies have dealt with the passage of test compounds. Caco-2 cells Caco-2 cells are the most popular cellular model in studies on passage and transport (Table II). They were derived from a human colorectal adenocarcinoma. In culture, they differentiate spontaneously into polarised intestinal cells possessing an apical brush border and tight junctions between adjacent cells, and they express hydrolases and typical microvillar transporters. This cell line was first used as a model for studying differentiation in the intestinal epithelium, and later for estimating the relative contributions of paracellular and transcellular passage in drug absorption. Caco-2 cells, despite their colonic origin, express in culture the majority of the morphological and functional characteristics of small intestinal absorptive cells, including phase I and phase II enzymes, detected either by measurement of their activities toward specific substrates, or by immunological techniques. However, CYP3A, which is present in almost all intestinal cells, is very weakly expressed in Caco-2 cells. Treatment with 1α,25-dihydroxyvitamin D3, an inducer of CYP3A4 at the mRNA level, and transfection of CYP3A4 cDNA, are two ways of increasing CYP3A expression levels in Caco-2 cells. However, these expression levels do not reach the levels observed in vivo (42, 43). With regard to phase II enzymes, Caco-2 cells express N-acetyl transferase and glutathione transferase activity. E. Le Ferrec et al. 656 Table II: Characteristics of parental Caco-2 cells Origin Human colorectal adenocarcinoma Growth in culture Monolayer epithelial cells Differentiation 14–21 days after confluence in standard culture medium Morphology Polarised cells, with tight junctions, apical brush border Electrical parameters High electrical resistance Digestive enzymes Typical membranous peptidases and disaccharidases of the small intestine Active transport Amino acids, sugars, vitamins, hormones . . . Membrane ionic transport Na+/K+ ATPase, H+/K+ ATPase, Na+/H+ exchange, Na+/K+/Cl– co-transport, apical Cl– channels Membrane non-ionic transporters Permeability-glycoprotein, multidrug resistant associated protein, lung cancer associated resistance protein Receptors Vitamin B12, vitamin D3, epidermal growth factor, sugar transporters (GLUT1, GLUT3, GLUT5, GLUT2, SGLT1) In addition, many groups have demonstrated the presence of P-gp activity in Caco2 monolayers, at levels higher than those found in the human colon in vivo (44, 45). The interpretation of transport data is therefore confusing, and is not always in agreement with in vivo observations, even when P-gp is blocked by specific inhibitors. Other membrane transporters, i.e. MRP and LRP, are also expressed (Table II). Interestingly, TC7 cells, isolated after the exposure of Caco-2 cells to methotrexate, express CYP3A at a higher level than their parental counterparts (Table III; 46). TC7 cells offer marked advantages over parental Caco-2 cells, because they express CYP3A, actively transport taurocolic acid, and have lower levels of P-gp compared with the parent Caco-2 cells. Several studies have demonstrated that TC7 cells are a good alternative to the Caco-2 parental line for drug transport studies (49). Caco-2 cells grow as a monolayer and differentiate on a semi-permeable membrane. Thus, separating the apical compartment from the basolateral compartment, which correspond to the intestinal lumen side and the serosal side, respectively, is possible (Figure 4). The complete morphological and functional differentiation of Caco-2 requires 3 weeks in culture under the conditions described in Table IV. Before using this model, various controls (summarised in Table V) have to be performed. Calculation of the permeability coefficient and interpretation of results In most cases, three parameters are determined: the apparent permeability (Papp), the flux, and the effective permeability (Peff). The coefficient of permeability is used in in vitro techniques, and the values are expressed as cm/second and are calculated by the following equation: ECVAM Workshop 46: the intestinal barrier Table III: Expression of mRNAs of various CYPs in Caco-2 and TC7 cells CYP Caco-2 TC7 + + + + + – + – + – + – + + + – 1A1 2B6 2C8/19 2D6 2E1 3A4 3A5 3A7 See reference (61). 657 Papp = dQ VdC = dT ⋅ A ⋅ C0 dT ⋅ A ⋅ C0 Equation 1 where V = sample volume (ml), dC = concentration variations, dQ = quantity variations, dT = time variations, C0 = the initial concentration in the donor compartment, and A = exposed surface (cellular monolayer in cm2). In the above formula, dQ/(dT ⋅ A) represents the mass transfer per unit time and unit surface across the monolayer. The effective permeability is used in in situ and organotypic techniques, and the values are calculated as follows: Peff = (Cin – Cout) ⋅ Qin Cout ⋅ 2πRL Equation 2 where Cin and Qin = the concentration and the quantity of compound at the entry of the Table IV: Culture conditions for use of Caco-2 cells in passage assays Inactivated serum in the medium on the apical site 20% Inactivated serum in the medium on the basolateral site 20% Coating Type 1 collagen (not required with 0.4µM filters) Not added under basal culture conditions Additive Non-essential amino acids Glucose Glutamine Antibiotics 1% 25mM 2mM Streptomycin (100µg/l) (optional) Penicillin (100mU/ml) (optional) CO2 10% or 5% pH Usually 7.4 at both sides or 7.4 in basolateral side and 6.5 in apical side (57) Cell density at seeding 2.5 × 105 – 4 × 105 cells/cm2 Number of passages 25–100 E. Le Ferrec et al. 658 Figure 4: A schematic respresentation of culture of Caco-2 cells on a microporous filter apical side microporous filter cell monolayer basolateral side intestinal segment, Cout = the concentration at the exit, R = the radius, and L = the length of the intestinal segment. The accuracy of measurements naturally depends upon the precision of dQ (Equation 1) or Cout (Equation 2). Moreover, Co (Equa- tion 1) and Cin (Equation 2) are limited by the solubility of the drug, the analytical sensitivity, and the effects of high drug concentrations on epithelial integrity. The classical method for studying transport from the apical to the basolateral sides Table V: Main controls for cell monolayers Transepithelial electrical resistance (TEER) Cell monolayer integrity. TEER measurement, depending on the filter area, can reveal a toxicity or an opening of tight junctions induced by the drug. For CaCo-2 cells, TEER values are 260–420Ω/cm2 (62–71); human intestine: 12–69 (64), rat ileum: 35 ± 4.9 (62); rat colon: 100 ± 26 (62). Differentiation markers By determination of sucrase-isomaltase, aminopeptidase and alkaline phosphatase activities Morphological differentiation By electron microscopy Permeability-glycoprotein (P-gp) expression By Western blotting or measurement of P-gp activity and by using immunohistochemistry Absence of contamination by mycoplasma Detection by standard microbiological methods Integrity of the cell monolayer by Mannitol, PEG 4000, lucifer yellow measuring permeability of test compounds ECVAM Workshop 46: the intestinal barrier 659 Figure 5: A schematic representation of the method used for measurement of transmembrane passage (apical [A] to basolateral [B]) of a drug in Caco2 cells transfer of support at different times support donor compartment (A) receiver compartment (B) relies on the transfer of the cell culture support at different times, as described in Figure 5. When samples are removed from the receiver chamber and replaced with control medium, a correction must be made to account for the corresponding dilution. The absence of effects of the drug on permeability characteristics and/or electrical parameters has to be verified (TEER measurement). A linear relationship between the A-to-B flux and the B-to-A flux at several concentration levels is an indication of a passive diffusion mode. A tight correlation between the flux (or Papp) and TEER is of significance in implying the paracellular route of drug transport. When the flux can be saturated, the occurrence of an energy-dependent and/or transporter-mediated transport is likely. In this case, the Michaëlis–Menten principles can be applied (for example, Km, Vmax). Many pharmacological tools exist that can explain transport mechanisms, for example, P-gp involvement, paracellular passage (Table VI). Comparison of the models Consistently good absorption is a key factor in selecting new drug candidates for development. In the discovery stage, drug absorption studies can be performed only in laboratory animals and/or in in vitro systems where the absorption process can be characterised both qualitatively and quantitatively. The various experimental protocols for predicting the fraction absorbed in humans from permeability coefficients have their own advantages and limitations (Table VII). The choice of model depends on compound availability, the stage of the project, and the questions to be answered. Drug absorption consists of passage through the epithelial layer and uptake into the bloodstream. In some models, such as the Ussing chamber or the everted gut sac, the drug must traverse all the intestinal wall, part of which might be rate-limiting in vitro, but not involved in vivo, thus leading to an underestimation of transport values. Cell lines, such as Caco-2, can be considered to be good models that mimic the physiological situation, as the drug traverses only the epithelial layer. However, it must be noted that one of the great differences between the in vivo situation and cell lines is the absence of mucus, which might limit absorption, especially that of lipophilic drugs. Moreover, cell monolayers contain only one cell type. Co-cultures consisting of cell lines with enterocytic markers (such as Caco-2 cells) and cell lines with mucus secretory functions (such as HT29MTX) have been proposed (47). Caco-2 monolayers have emerged as a suitable model for studying drug absorption (Table VIII). Most studies with Caco-2 monolayers were performed to determine whether a drug is actively or passively transported across the intestinal epithelium, and to pro- E. Le Ferrec et al. 660 vide new insights into the regulation of drug transport. However, the predictions of absorption in humans based on permeability data obtained with Caco-2 monolayers from different laboratories are not satisfactory. For example, Artursson & Karlsson (48) have compared the passage of 20 structurally unrelated drugs in Caco-2 cell monolayers with the extent of absorption in humans after oral administration, and concluded that drugs having a complete absorption in humans were found to have a high permeability coefficient (Papp ≥ 1 × 10–6cm/s) in Caco-2 cells, whereas poorly absorbed drugs had a low permeability coefficient (Papp < 1 × 10–7cm/s). However, similar studies (49, 50) did not lead to the same results (Table IX). The reasons for such a discrepancy between laboratories in the reported permeability values are not clear. Such results indicate that, although Caco2 monolayers are a useful model for ranking drugs according to their permeability, they cannot be used to quantitatively predict human absorption in vivo. As an example, Gan et al. (51) reported that the Caco-2 permeability coefficient of ranitidine was 1 × 10–7cm/s (i.e. corresponding to a low permeability), whereas the human bioavailability of this drug is good (50–70%). Other attempts have been made to compare in vitro and in vivo drug permeability Table VI: Pharmacological agents for use in passage studies Mechanism Agents P-gp involvement Inhibitor MRP involvement LRP involvement Verapamil ≤ 0.5mM in apical (A) and basolateral (B) sides Quinidine 0.5–1mM in A and B Cyclosporin A 50µM in A and B Substrate Rhodamine 123 1mM Inhibitor As for substrates Substrate Leucotriene C4, S-2,4-dinitrophenyl glutathione, PAH, doxorubicin, etoposide, vinblastine, methotrexate Increase the transport from the apical side to the basolateral side (if the drug is added on the apical side) Efflux of rhodamine at the apical side Inhibitor Substrate Paracellular transport (by action on tight junctions) Effects Anthracycline EGTA, cytochalasine Increase the transport, if paracellular P-gp = permeability glycoprotein, MRP = multidrug resistance associated protein, LRP = lung cancer associated resistance protein. It is a reference model. A difficult technique with local anaesthesia at the time All physiological factors that influence passage are present. of catheter introduction. Allows studies in humans. Not used either in development or routinely. Good correlation with pharmacokinetic studies. All cell types and the mucous layer are present. A relatively fast and inexpensive technique. Can be used for mechanism of absorption or formulation studies. Drug absorption and passage at specific intestinal sites are possible. The test drug can be added on either the apical or the basolateral side. Metabolism studies are possible. A human and animal model. Human intestinal perfusion Intestinal gut sac (rat) Ussing chamber (human, rat) Measurement techniques must be sensitive, since the drugs are diluted in the diffusion chambers. Cell viability is limited. The drug must cross the whole intestinal wall. Availability of human tissue is limited. Not used for screening. Not a perfused model. The drug must cross the whole intestinal wall. It is an animal model. Used in development, but not routinely. The increase of luminal hydrostatic pressure during the experiment can influence intestinal permeability. It is an animal model. Integrates passage and metabolism aspects. All physiological factors that influence passage are present. Studies of absorption in particular sites of the intestine are possible. Studies of direct effects of the drug on intestinal absorption are possible. In situ technique (rat) Limitations Advantages Techniques Table VII: Advantages and limitations of the various models Relatively fast and simple method. A flexible model. Can be used for mechanism transport studies. The test drug can be exposed at the apical or the basolateral side. Human cells. Can be used for drug screening testing. Express CYP3A. Growth faster than that of Caco-2 cells. Need less glucose than Caco-2 cells. Fast and simple method. Can be used for screening testing. Can be used for measurement of passive diffusion. Do not express P-gp. Caco-2 cells TC7 cells MDCK cells Cell culture P-gp = permeability glycoprotein; MDCK = Madin Darby canine kidney. Advantages Techniques Table VII: continued Not an intestinal model. It is an animal model. Physiological factors that influence passage are not present (mucous, bile salts, cholesterol). A static model. Cells have a tumoral origin. A model with only one cell type. Influence of P-gp difficult to estimate. Limitations ECVAM Workshop 46: the intestinal barrier 663 Table VIII: Examples of mechanistic and drug absorption studies using Caco-2 cells Route of passage Factor influencing drug absorption Model used References Paracellular Molecular size Flexibility of drug geometric structure Caco-2 Caco-2 (65) (62) Transcellular Lipophilicity Hydrogen bond Caco-2 Caco-2 (63, 71) (66, 67) (Table X). Comparison of the permeability coefficients of a series of drugs by using Caco-2 cells and the double-balloon technique in the human jejunum (52, 53), showed that the permeability of drugs with complete absorption differed by two-fold to four-fold between the in vitro and in situ models, whereas the permeability of drugs with poor absorption differed as much as 30-fold to 80fold. Thus, measurement of permeability by using Caco-2 cells allows only a qualitative comparison. Moreover, correlations between the different techniques are better when the mode of passage is passive diffusion (6, 25, 50, 54). When a receptor-mediated molecular transport is involved, the calculation of correlation coefficients is difficult, or even impossible. Because the properties of Caco-2 monolayers can vary with time in culture, passage number and culture medium composition, it is important to include a reference drug when screening for the permeability of test drugs. Table IX: It should also be borne in mind that monolayers constitute a two-dimensional system, whereas the intestinal mucosa is a threedimensional one, i.e. it is not flat, but convoluted because of villi and folds. Depending on the actual available surface area for absorption, the estimates are made difficult by the calculation of the permeability coefficient, where the surface area of the tube (the balloon technique) is used. The actual surface might be larger; hence, the reported permeability would be too high. Since in vitro models cannot give quantitative predictions of drug absorption in humans, another possibility is to use animal models (49). This is based on the assumption that the membrane permeability of drugs is not species-dependent (55). Since the composition of the plasma membrane of intestinal epithelial cells is similar across species, the permeability of drugs (simple diffusion) across the wall of the gastrointestinal tract could be expected to be similar (Table X). Drug absorption in humans can be extrapo- Permeability limit values proposed by several authors using Caco-2 cells (56) Apparent permeability in Caco-2 cells Low permeability limit values High permeability limit values Reference ≤ 1 × 10–7cm/second < 1 × 10–5cm/second ≥ 1 × 10–6cm/second > 7 × 10–5cm/second > 3 × 10–5cm/second (48) (64) (50) 20 20 20 12 12 10 16 12 TC7 vs Caco-2 cells (68) Caco-2 cells vs human oral route (48, 68, 69) TC7 cells vs human oral route (68) “Rat” Ussing chamber vs “human” Ussing chamber (70) “Rat” Ussing chamber vs oral route in humans (70) “Rat” in situ perfusion vs “human” in situ perfusion (53) “Rat” in situ perfusion vs human oral route (50) “Rat” intestinal gut sac vs human oral route (50) For preliminary screening. For small organic molecules. High correlation exists between the two models for passively absorbed molecules. The two models can be used to predict absorption in humans. A marker should be included in the “rat model” to follow viability. The “rat” Ussing chamber technique is especially useful for screening substances having local pharmacological and transporter-mediated effects. Caco-2 and TC7 cells are used for the prediction of passive human passage. Caco-2 and TC7 cells are used for the prediction of passive human passage. Based on morphological and biochemical parameters and also on transport characteristics, it appears that TC7 cells are a reliable alternative to Caco-2 parental lines for transport studies. The Papp correlation coefficient calculated by these two techniques is 0.79. Moreoever, comparison of the Papp values calculated in MDCK and Caco-2 cells in relation to the human oral route is 0.58 and 0.54, respectively, indicating that both cells are suitable. Comment + +++ +++ +++ ++ +++ +++ +++ ++ Correlation poly(ethylene glycol) (PEG), furosemide, propranolol, atenolol, metoprolol, terbutaline, enalapril, L-dopa, D-mannitol D-Glucose, Currently tested compounds + = limited correlation, ++ = median correlation, +++ = high correlation. MDCK = Madin Darby canine kidney. Papp = apparent permeability. 55 Caco-2 vs MDCK cells (55) Technique Number of compounds tested Table X: Correlations between various techniques ECVAM Workshop 46: the intestinal barrier Class II low solubility high permeability Class I high solubility high permeability Class IV low solubility low permeability Class III high solubility low permeability solubility Figure 7: In vitro/in vivo correlation permeability permeability Figure 6: Biopharmaceutical classification system (57) 665 correlationb Class IV no expected correlation Class III low or no correlation solubility a If the dissolution rate is slower than the gastric emptying rate, otherwise limited or no correlation. See ref. 57. b lated reasonably well from animal data, when information on first-pass metabolism is also available (56). Bioavailability, however, differs substantially among species, presumably as a result of species differences in the scale of first-pass metabolism. The United States Pharmacopeial Convention (USP) has proposed two schemes for predicting in vivo and in vitro correlations. Figure 6 illustrates in vivo/in vitro correlations for molecules classified according to solubility and permeability. Figure 7 illustrates correlations between in vivo and in vitro data. It shows that highly permeable molecules (classes I and II) exhibit a high in vivo/in vitro correlation, whereas poorly permeable molecules (classes III and IV) show a low in vivo/in vitro correlation. The USP proposes the selection of reference molecules with known Papp values (methotrexate: 1.2 × 10–6cm/s; propranolol hydrochloride: 28 × 10–6cm/s; testosterone: 73 × 10–6cm/s). If the Papp values obtained with Caco-2 cells are the same as the Papp values given by the USP (± 20%), the model can be considered to be valid (57). However, because the USP defines rigid limits, such recommendations are not accepted by all users. Many researchers prefer to use a collection of laboratory values, with internal specifications and criteria of acceptance for each assay system. Another approach chosen by some researchers is to delineate the correlationa If in vivo and in vitro dissolution rates are similar (57). physicochemical properties that favour intestinal absorption, and they have developed computational methods for their prediction. The best-known method is probably the “rule of five” designed by Lipinski and coworkers (58) from an analysis of 2245 drugs. As implemented in their system, the “rule of five” generates an alert (an indication of possible absorption problems) for compounds, when: 1) there are more than five hydrogenbond donors (expressed as the sum of hydroxyl and primary amine groups); 2) the molecular mass is over 50; 3) the Log P is over 5 (or MlogP is over 4.15); 4) there are more than ten hydrogen-bond acceptors (expressed as the sum of nitrogen and oxygen atoms); and 5) compound classes that are substrates for biological transporters are exceptions to the rule. The “rule of five” method was originally proposed because many of the large numbers of hit compounds selected by HTS did not possess “drug-like” properties. Obviously, the growing number of publications in this field indicate that methods for predicting “drug-likeness” are already having a major impact on the design and selection of compounds in pharmaceutical companies. The routine use of experimental absorption systems in the pre-screening of compounds is providing valuable data, and should permit E. Le Ferrec et al. 666 the development of improved models for drug absorption. The value of such experimental and theoretical systems will become apparent when drug development times are reduced. 5. 6. Conclusions and Recommendations 1. Knowledge on P-gp expression in human intestine and cell lines should be improved. 2. Cell lines other than Caco-2 (for example, HT29, TC7, 2/4/A1) should be more fully investigated. 3. The absence of mucus in cell lines is a problem. Co-culturing cell lines expressing enterocytic markers (for example, Caco-2 cells) with cell lines exhibiting mucus secretory properties (for example, the HT-29 cell line [59]) could permit this limitation to be overcome. 4. 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